Peres, P. A. | bioRxiv Science

bioRxiv2025

Phylogenomics supports monophyly of marsupial crustaceans: a journey to direct development

Peracarida (marsupial crustaceans) represent one of the most diverse and ecologically important crustacean groups, yet their evolutionary relationships have long been debated. Here, we present the most comprehensive phylogenomic analysis of Peracarida to date, incorporating the relict taxa Thermosbaenacea, Mictacea, Ingolfiellida, and Spelaeogriphacea for the first time in a phylogenomic framework. Our results robustly confirm peracarid monophyly and recover a well-supported clade uniting Mancoida (Isopoda, Tanaidaca, Cumacea), Mictacea, and Spelaeogriphacea. We propose the new taxon Panmancoida to encompass this expanded lineage defined by shared developmental and morphological traits. The inferred phylogeny further suggests that peracarid evolution involved a transition from an intermediate "pseudodirect" developmental mode to the direct development seen in most lineages. We further show that the shift to extensive brood care within the marsupium, accompanied by the loss of a free-swimming larval stage, may have accelerated rates of molecular evolution across lineages. Together, these findings provide a robust evolutionary framework for this major malacostracan lineage and highlight how key reproductive innovations reshaped the genomic and life-history trajectories of the marsupial crustaceans.

evolutionary biology↗

bioRxiv2024

Water volume, biological and PCR replicates influence the characterization of deep-sea pelagic fish communities.

The pelagic deep sea is challenging to investigate due to logistical constraints regarding access and collection of samples, however environmental DNA (eDNA) can potentially revolutionize our understanding of this ecosystem. Although recent advancements are being made regarding eDNA technology and autonomous underwater vehicles, no investigation has been performed to assess the impact of different experimental designs using gear found on many research vessels (i.e., CTD mounted with Niskin bottles). Here, we investigated the effects of sampled water volume, biological and PCR replicates in characterizing deep-sea pelagic biodiversity at the level of species and exact sequence variants (ESVs, representing intraspecific variation). Samples were collected at 450m depth at night in the northern Gulf of Mexico using Niskin bottles, and we targeted the fish community using the MiFish primer (12S rRNA). Our results show that 1L is insufficient to characterize deep-sea pelagic fish communities. The 5L and 10L treatments detected similar community structure (i.e., the combination of number of species and relative occurrence) and numbers of species per biological replicate, but the 10L treatment detected a higher total number of species, more ESVs, and a different community structure when considering ESVs. We found that five biological replicates can detect up to 80% of the species detected in this study in the water collected in both 5L and 10L treatments. PCR replicates also had an important role in species and ESV detection, which implies increasing PCR replicates if water volume is limited. We suggest that future studies collect at least 5L, 5 or more field replicates, and 5-10 PCR replicates to adequately investigate deep-sea pelagic biodiversity using eDNA, considering resource limitations. Our study provides guidance for future eDNA studies and a potential route to expand eDNA studies at a global scale.

ecology↗